Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-5960
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dc.contributor.authorLoos, Julia-
dc.contributor.authorPfeuffer, Steffen-
dc.contributor.authorPape, Katrin-
dc.contributor.authorRuck, Tobias-
dc.contributor.authorLüssi, Felix-
dc.contributor.authorSpreer, Annette-
dc.contributor.authorZipp, Frauke-
dc.contributor.authorMeuth, Sven G.-
dc.contributor.authorBittner, Stefan-
dc.date.accessioned2021-05-31T10:17:44Z-
dc.date.available2021-05-31T10:17:44Z-
dc.date.issued2020-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/5969-
dc.description.abstractBACKGROUND Based on clinical, immunological and histopathological evidence, MOG-IgG-associated encephalomyelitis (MOG-EM) has emerged as a distinct disease entity different from multiple sclerosis (MS) and aquaporin-4-antibody-positive neuromyelitis optica spectrum disorder (NMOSD). MOG-EM is associated with a broader clinical phenotype including optic neuritis, myelitis, brainstem lesions and acute disseminated encephalomyelitis with a substantial clinical and radiological overlap to other demyelinating CNS disorders. OBJECTIVE To evaluate common clinical, MRI and CSF findings, as well as therapy responses in patients with longitudinal extensive transverse myelitis (LETM) as initial clinical presentation of MOG-EM. METHODS After excluding patients with a known diagnosis of MS, we identified 153 patients with myelitis of which 7 fulfilled the inclusion criteria and were investigated for MRI, CSF and clinical parameters. RESULTS Patients with LETM as first clinical presentation of MOG-EM display similar characteristics, namely a lack of gadolinium-enhancement in spinal cord MRI, marked pleocytosis, negative oligoclonal bands, a previous history of infections/vaccinations and response to antibody-depleting treatments for acute attacks and long-term treatment. CONCLUSIONS We identify common pathological findings in patients with LETM as first clinical presentation of MOG-EM which distinguishes it from other forms of LETM and should lead to testing for MOG-IgG in these cases.en_GB
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleMOG encephalomyelitis: distinct clinical, MRI and CSF features in patients with longitudinal extensive transverse myelitis as first clinical presentationen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-5960-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleJournal of neurologyde
jgu.journal.volume267de
jgu.pages.start1632de
jgu.pages.end1642de
jgu.publisher.year2020-
jgu.publisher.nameSpringerde
jgu.publisher.placeHeidelbergde
jgu.publisher.urihttps://doi.org/10.1007/s00415-020-09755-xde
jgu.publisher.issn1432-1459de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.1007/s00415-020-09755-x
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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